- Trials with a EudraCT protocol (124)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
124 result(s) found for: Adiposity.
Displaying page 1 of 7.
EudraCT Number: 2007-001787-71 | Sponsor Protocol Number: CCB-CRC-07-01 | Start Date*: 2008-02-11 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: The influence of Rimonabant induced cannabinoid receptor blocking on the mass and function of the left ventricle in patients with abdominal adiposity | ||
Medical condition: Adiposity is another risk factor for developing cardiac insufficiency and myocardial hypertrophy. Probably the volume loading of the left ventricle, systemic inflammation, the fatty degeneration of... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-001048-22 | Sponsor Protocol Number: 990312 | Start Date*: 2005-12-29 |
Sponsor Name:Göteborg University, Institute for Internal Medicine | ||
Full Title: Rosuvastatin in Visceral Adiposity. A 26-week, single center, randomised, placebo-controlled, double-blind, parallel-group study to evaluate the effect of rosuvastatin on visceral adipose tissue in... | ||
Medical condition: Visceral adiposity | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003740-89 | Sponsor Protocol Number: MR-Som-01-20 | Start Date*: 2020-11-26 | |||||||||||
Sponsor Name:SOCIETÀ ITALO BRITANNICA L. MANETTI - H. ROBERTS & C. PER AZIONI | |||||||||||||
Full Title: A Phase IV, interventional, monocentric, not controlled study for the evaluation of new clinical and instrumental parameters on the efficacy of SOMATOLINE in the treatment of local adiposity and ce... | |||||||||||||
Medical condition: local adiposity and cellulite | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000223-85 | Sponsor Protocol Number: 140631 | Start Date*: 2015-04-09 |
Sponsor Name:Örebro University Hospital | ||
Full Title: The effects of Vitamin D supplementation on cardiorespiratory fitness and adiposity in overweight men. A randomised, double-blind, placebo controlled study. | ||
Medical condition: We aim to examine the effects of Vitamin D supplementation on cardiorespiratory fitness and adiposity in overweight men. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003910-26 | Sponsor Protocol Number: 01/2015 | Start Date*: 2017-12-11 |
Sponsor Name:Núcleo de Estudos de Hipertensão da Beira Interior | ||
Full Title: Fase II, unicenter, open, randomized trial to evaluate the response of Th17 and T regulatory lymphocytes to 24 weeks supplementation with cholecalciferol in patients with arterial hypertension, obe... | ||
Medical condition: Obesity associated arterial hypertension Metabolic syndrome associated arterial hypertension | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-003816-47 | Sponsor Protocol Number: Met-ADI-01 | Start Date*: Information not available in EudraCT |
Sponsor Name:Pädiatrische Endokrinologie, Universitätsmedizin Berlin, Charité | ||
Full Title: Clinical pilot study on the effect of Metformin in adipose children and adolescents with insulin-resistance Klinische Pilotstudie zur Untersuchung der Wirkung von Metformin bei adipösen Kindern un... | ||
Medical condition: Insuline-resistance in adipose children and adolescents | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006082-88 | Sponsor Protocol Number: Rimonamaag | Start Date*: 2008-10-21 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: INFLUENCE OF RIMONABANT ON GASTRIC SENSITIVITY AND ON THE GASTRIC RESPONSE TO A MEAL IN HEALTHY VOLUNTEERS | |||||||||||||
Medical condition: none; this is a physiological study to investigate the influence of CB1 receptor antagonism by rimonabant (normally used for the treatment of obesity) on gastric sensorimotor function | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004292-11 | Sponsor Protocol Number: DISCO001 | Start Date*: 2005-10-06 |
Sponsor Name:Endocrine Department, Sahlgrenska University Hospital | ||
Full Title: Discontinuation of long-term GH replacement therapy - a randomised, placebo controlled trial in adult GH deficiency. | ||
Medical condition: This is a study in growth hormone deficient adult patients on stable growth hormone therapy of discountinuate growth hormone (GH) for 4 months in double blinded crossover, palcebo/controlled, rand... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003387-12 | Sponsor Protocol Number: DopamineGenetics01 | Start Date*: 2018-03-15 | |||||||||||||||||||||
Sponsor Name:University Hospital Tuebingen | |||||||||||||||||||||||
Full Title: Dopamine action on metabolism depending on genetic heterogeneity – a randomized, placebo-controlled double blind study | |||||||||||||||||||||||
Medical condition: Adipositas ist eine weit verbreitete und in ihrer Prävalenz zunehmende Erkrankung, die mit schwerwiegenden Folgeerkrankungen einhergeht. Von häufigen genetischen Polymorphismen haben Varianten im F... | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001840-38 | Sponsor Protocol Number: BET207 | Start Date*: 2008-08-05 | |||||||||||
Sponsor Name:OBEcure | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Examine the Effect of Betahistine on Body Weight in Obese Female Subjects | |||||||||||||
Medical condition: obesity | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002712-51 | Sponsor Protocol Number: 2020 | Start Date*: 2021-03-05 | |||||||||||
Sponsor Name:Kirsi Pietiläinen | |||||||||||||
Full Title: Semaglutide as an adjunct to dieting in the treatment of type 2 diabetes – effects on glucose metabolism, prevention of weight regain and peripheral tissue metabolic activation | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003908-61 | Sponsor Protocol Number: Vasc-UMCU-10B | Start Date*: 2008-12-09 | |||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||
Full Title: A MULTICENTER, DOUBLE-BLIND, RANDOMIZED, 2-PERIOD, CROSSOVER STUDY TO COMPARE THE EFFECTS OF EZETIMIBE/SIMVASTATIN (10 MG/10 MG) COMBINATION TABLET VERSUS SIMVASTATIN 80 MG TABLET ON POSTPRANDIAL A... | |||||||||||||
Medical condition: Metabolic syndrome as defined by the ATP III criteria | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006424-18 | Sponsor Protocol Number: EC/2006/117/PGMS | Start Date*: 2007-03-01 | |||||||||||
Sponsor Name:University of Surrey | |||||||||||||
Full Title: THE EFFECT OF RIMONABANT ON ENERGY EXPENDITURE, FATTY ACID METABOLISM, TRIACYLGLYCEROL METABOLISM AND BODY FAT DISTRIBUTION | |||||||||||||
Medical condition: Obesity | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002862-20 | Sponsor Protocol Number: NS2330-001 | Start Date*: 2006-08-03 | |||||||||||
Sponsor Name:NeuroSearch A/S | |||||||||||||
Full Title: Effect of tesofensine on weight reduction in patients with obesity. A randomised, double-blind, placebo-controlled, parallel-group, multi-centre study. | |||||||||||||
Medical condition: Obesity | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003293-93 | Sponsor Protocol Number: 14072011 | Start Date*: 2011-09-23 |
Sponsor Name:Sint Antonius Ziekenhuis | ||
Full Title: Cyp3A4 metabolism before and after surgery induced weight loss in morbidly obese patients, using midazolam as a model drug | ||
Medical condition: Morbid obesity | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001121-10 | Sponsor Protocol Number: NS2330-004 | Start Date*: 2007-05-10 | |||||||||||
Sponsor Name:NeuroSearch A/S | |||||||||||||
Full Title: Evaluation of long term safety of tesofensine in patients with obesety. | |||||||||||||
Medical condition: Obesity | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002755-42 | Sponsor Protocol Number: 1069/12 | Start Date*: 2012-11-06 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: OBESITY AND ASPIRIN RESPONSIVENESS | |||||||||||||
Medical condition: OBESITY | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004951-35 | Sponsor Protocol Number: DISOBBED-12 | Start Date*: 2013-01-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
Full Title: Disulfiram, obesity and binge eating disorder | |||||||||||||
Medical condition: Obesity and binge eating disorder | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001869-29 | Sponsor Protocol Number: 2515/2008 | Start Date*: 2008-08-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Mechanism of action and metabolic effects of exenatide in obesity | |||||||||||||
Medical condition: no diabetic, obese subjects with BMI≥40 kg.m-2 | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003244-30 | Sponsor Protocol Number: no sponsor | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Rijnstate Hospital | |||||||||||||
Full Title: Diazoxide-Mediated Insulin Suppression in Hyperinsulinemic Obese Men, part III. | |||||||||||||
Medical condition: Hyperinsulinemic men with BMI 30-35 kg/m2 | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
• EEA CTAs: Date study was authorised to proceed
• Outside EU/EEA: Date study was submitted in EudraCT
• Outside EU/EEA: Date study was submitted in EudraCT
